SCHEMBL1774094

SCHEMBL1774094

O=c1[nH]ccc2sc(Br)cc12

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 5/20 0.43
ALDH1A1 P00352 2/20 0.35
KDM4E B2RXH2 1/20 0.35
LMNA P02545 1/20 0.35
CYP1A2 P05177 1/20 0.35
CYP3A4 P08684 1/20 0.35
CYP2C9 P11712 1/20 0.35
HPGD P15428 1/20 0.35
RAB9A P51151 1/20 0.35
BLM P54132 1/20 0.35
PARP15 Q460N3 1/20 0.35
HSD17B10 Q99714 1/20 0.35
RECQL P46063 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
GSK3B P49841 2/20 0.33
GRM5 P41594 1/20 0.33
CHEK1 O14757 6/20 0.33
PIM1 P11309 1/20 0.33
AKT1 P31749 1/20 0.33
FLT3 P36888 1/20 0.33

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL7835046 0.78 PARP1 (0.39) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL4341520 0.77 ALDH1A1 (0.47) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL15716637 0.74 CYP2A6 (0.42) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL7058856 0.73 MCL1 (0.38) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL22323693 0.73 MGLL (0.41) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL5849531 0.73 TMIGD3 (0.51) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL15728254 0.73 PARP1 (0.35) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL20586642 0.73 CYP2A6 (0.41) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL12219884 0.73 PARP1 (0.35) PARP1ALDH1A1KDM4ELMNACYP1A2
SCHEMBL10647302 0.72 CA2 (0.53) PARP1ALDH1A1KDM4ELMNACYP1A2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 65 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260092053-A1 KHK INHIBITORS GILEAD SCIENCES INC (US) 2026-04-02 US disclosed
EP-4681774-A2 KHK INHIBITORS Gilead Sciences, Inc. (US) 2026-01-21 EP disclosed
US-12528825-B2 Compounds and uses thereof FOGHORN THERAPEUTICS INC. (US) 2026-01-20 US disclosed
US-12509460-B2 Methods and compositions for modulating splicing SKYHAWK THERAPEUTICS, INC. (US) 2025-12-30 US disclosed
EP-4313967-B1 KHK INHIBITORS GILEAD SCIENCES INC (US) 2025-11-12 EP disclosed
US-20250276978-A1 HETEROCYCLIC COMPOUNDS AS BET INHIBITORS SAGARD HOLDINGS MANAGER LP, AS ADMINISTRATIVE AGENT (CA) 2025-09-04 US disclosed
US-20250144094-A1 THIOPHENE ULK1/2 INHIBITORS AND THEIR USE THEREOF ERASCA, INC. 2025-05-08 US disclosed
US-12227515-B2 In-flow photooxygenation of aminothienopyridinones generates novel PTP4A3 phosphatase inhibitors UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2025-02-18 US disclosed
US-12202839-B2 In-flow photooxygenation of aminothienopyridinones generates PTP4A3 phosphatase inhibitors UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2025-01-21 US disclosed
EP-4433059-A1 THIOPHENE ULK1/2 INHIBITORS AND THEIR USE THEREOF Erasca, Inc. (US) 2024-09-25 EP disclosed
EP-2920183-A1 THIENO[3,2-C]PYRIDIN-4(5H)-ONES AS BET INHIBITORS Glaxosmithkline LLC (US) 2015-09-23 EP disclosed
WO-2014078257-A1 THIENO[3,2-C]PYRIDIN-4(5H)-ONES AS BET INHIBITORS GLAXOSMITHKLINE LLC (US) 2014-05-22 WO disclosed
WO-2014078257-A1 THIENO[3,2-C]PYRIDIN-4(5H)-ONES AS BET INHIBITORS GLAXOSMITHKLINE LLC (US) 2014-05-22 WO disclosed
US-7943639-B2 Such as 6-benzenesulfonyl-4-piperazin-1-yl-quinoline hydrochloride; for treatment of central nervous system and/or 5- HT6 receptor related disorders; for weight gain/loss PROXIMAGEN LIMITED (GB) 2011-05-17 US disclosed
US-7943639-B2 Such as 6-benzenesulfonyl-4-piperazin-1-yl-quinoline hydrochloride; for treatment of central nervous system and/or 5- HT6 receptor related disorders; for weight gain/loss PROXIMAGEN LIMITED (GB) 2011-05-17 US disclosed
EP-1897881-A2 Compounds useful for the treatment of obesity, type II diabetes and CNS disorders Biovitrum AB (publ) (SE) 2008-03-12 EP disclosed
EP-1556053-A4 ANTIINFLAMMATION AGENTS AMGEN INC (US) 2006-04-19 EP disclosed
EP-1556053-A1 ANTIINFLAMMATION AGENTS Amgen Inc. (US) 2005-07-27 EP disclosed
WO-2004041285-A1 ANTIINFLAMMATION AGENTS AMGEN INC. (US) 2004-05-21 WO disclosed
US-20040024210-A1 New compounds PROXIMAGEN NEUROSCIENCE PLC (GB) 2004-02-05 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250144094-A1 THIOPHENE ULK1/2 INHIBITORS AND THEIR USE THEREOF ULK1, ULK2, ULK3 PARP1 869/4885ALDH1A1 3129/4885KDM4E 1266/4885
US-20250276978-A1 HETEROCYCLIC COMPOUNDS AS BET INHIBITORS BET1, BRD4, BRD3 PARP1 408/4885ALDH1A1 4239/4885KDM4E 555/4885
US-12509460-B2 Methods and compositions for modulating splicing SF3B1, RTCB, RBM17 PARP1 2329/4885ALDH1A1 3032/4885KDM4E 2036/4885
US-20040024210-A1 New compounds SULT1E1, SULT2A1, SULT1A1 PARP1 4152/4885ALDH1A1 705/4885KDM4E 2527/4885
US-20260092053-A1 KHK INHIBITORS KHK, SLC5A2, HK1 PARP1 4713/4885ALDH1A1 700/4885KDM4E 684/4885
US-12202839-B2 In-flow photooxygenation of aminothienopyridinones generates PTP4A3 phosphatase inhibitors PTP4A3, PTPRO, PTPRC PARP1 1151/4885ALDH1A1 1667/4885KDM4E 176/4885
US-12528825-B2 Compounds and uses thereof BRD9, BRD8, BRIX1 PARP1 2033/4885ALDH1A1 4477/4885KDM4E 574/4885
US-12227515-B2 In-flow photooxygenation of aminothienopyridinones generates novel PTP4A3 phosphatase inhibitors PTP4A3, PTPRC, PTPRF PARP1 1313/4885ALDH1A1 1620/4885KDM4E 241/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.